SUNMASTER

GUDID G5101981

Light Sources, Inc.

Ultraviolet tanning device

• Primary Device ID: G5101981
• NIH Device Record Key: e8a93ad8-0335-4e03-8aaf-64a0f6953de0
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SUNMASTER
• Version Model Number: 1981
• Company DUNS: 075058495
• Company Name: Light Sources, Inc.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	G5101981 [Primary]

FDA Product Code

• LEJ: Booth, Sun Tan

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-01-22
• Device Publish Date: 2025-01-14

On-Brand Devices [SUNMASTER]

• G5102714: FR71T12/BL/HO/BP/6.5B
• G5102715: 2715
• G5102168: 2168
• G5101981: 1981
• G5101957: 1957
• G51027770: 2777
• G5102191: 2191